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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7098705complex chromosomal rearrangement16nstd230human GRCh37 chr6: 152,298,852-152,298,852 , GRCh37 chr6: 152,298,855-152,298,855 , GRCh37 chr6: 152,461,093-152,461,093 , GRCh37 chr6: 152,461,093-152,461,093 , GRCh37 chr6: 152,690,618-152,690,618 , GRCh37 chr6: 152,690,827-152,690,827 , GRCh37 chr6: 152,692,590-152,692,590 , GRCh37 chr6: 152,692,596-152,692,596 , GRCh37 chr6: 152,692,616-152,692,616 , GRCh37 chr6: 152,692,620-152,692,620 , GRCh37 chr6: 152,697,228-152,697,228 , GRCh37 chr6: 152,697,240-152,697,240 , GRCh37 chr6: 153,511,451-153,511,451 , GRCh37 chr6: 153,511,464-153,511,464 , GRCh37 chr6: 153,511,478-153,511,478 , GRCh37 chr6: 153,511,479-153,511,479 , GRCh37 chr6: 153,621,313-153,621,313 , GRCh37 chr6: 153,621,317-153,621,317 , GRCh37 chr6: 153,863,854-153,863,854 , GRCh37 chr6: 153,863,854-153,863,854 , GRCh37 chr13: 82,735,924-82,735,924 , GRCh37 chr13: 82,735,928-82,735,928 , GRCh37 chr13: 87,918,047-87,918,047 , GRCh37 chr13: 87,918,061-87,918,061 , GRCh37 chr13: 107,614,717-107,614,717 , GRCh37 chr13: 107,614,717-107,614,717 , GRCh37 chr13: 107,657,183-107,657,183 , GRCh37 chr13: 107,657,185-107,657,185 , GRCh37 chr15: 98,510,600-98,510,600 , GRCh37 chr15: 98,510,601-98,510,601 , GRCh37 chr16: 26,210,170-26,210,170 , GRCh37 chr16: 26,210,189-26,210,189 , GRCh38.p12 chr15: 97,967,370-97,967,370 , GRCh38.p12 chr15: 97,967,371-97,967,371 , GRCh38.p12 chr16: 26,198,849-26,198,849 , GRCh38.p12 chr16: 26,198,868-26,198,868 , GRCh38.p12 chr6: 151,977,717-151,977,717 , GRCh38.p12 chr6: 151,977,720-151,977,720 , GRCh38.p12 chr6: 152,139,958-152,139,958 , GRCh38.p12 chr6: 152,139,958-152,139,958 , GRCh38.p12 chr6: 152,369,483-152,369,483 , GRCh38.p12 chr6: 152,369,692-152,369,692 , GRCh38.p12 chr6: 152,371,455-152,371,455 , GRCh38.p12 chr6: 152,371,461-152,371,461 , GRCh38.p12 chr6: 152,371,481-152,371,481 , GRCh38.p12 chr6: 152,371,485-152,371,485 , GRCh38.p12 chr6: 152,376,093-152,376,093 , GRCh38.p12 chr6: 152,376,105-152,376,105 , GRCh38.p12 chr6: 153,190,316-153,190,316 , GRCh38.p12 chr6: 153,190,329-153,190,329 , GRCh38.p12 chr6: 153,190,343-153,190,343 , GRCh38.p12 chr6: 153,190,344-153,190,344 , GRCh38.p12 chr6: 153,300,178-153,300,178 , GRCh38.p12 chr6: 153,300,182-153,300,182 , GRCh38.p12 chr6: 153,542,719-153,542,719 , GRCh38.p12 chr6: 153,542,719-153,542,719 , GRCh38.p12 chr13: 82,161,789-82,161,789 , GRCh38.p12 chr13: 82,161,793-82,161,793 , GRCh38.p12 chr13: 87,265,792-87,265,792 , GRCh38.p12 chr13: 87,265,806-87,265,806 , GRCh38.p12 chr13: 106,962,369-106,962,369 , GRCh38.p12 chr13: 106,962,369-106,962,369 , GRCh38.p12 chr13: 107,004,835-107,004,835 , GRCh38.p12 chr13: 107,004,837-107,004,837 ESR1, SYNE1, 1 more genes
    nsv7056989inversion1nstd229human GRCh38 chr6: 151,827,345-151,827,472 , GRCh37.p13 chr6: 152,148,480-152,148,607 ESR1
    nsv7054669inversion1nstd229human GRCh38 chr6: 151,926,018-151,935,594 , GRCh37.p13 chr6: 152,247,153-152,256,729 ESR1
    nsv7052756inversion1nstd229human GRCh38 chr6: 151,867,288-151,933,047 , GRCh37.p13 chr6: 152,188,423-152,254,182 ESR1
    nsv7048058inversion1nstd229human GRCh38 chr6: 151,871,215-151,871,250 , GRCh37.p13 chr6: 152,192,350-152,192,385 ESR1
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv7042383inversion1nstd229human GRCh38 chr6: 151,557,708-151,652,382 , GRCh37.p13 chr6: 151,878,843-151,973,517 ESR1, CCDC170, 2 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv7040284inversion1nstd229human GRCh38 chr6: 151,871,236-151,871,280 , GRCh37.p13 chr6: 152,192,371-152,192,415 ESR1
    nsv6817471copy number variation1nstd229human GRCh38 chr6: 152,068,859-152,071,098 , GRCh37.p13 chr6: 152,389,994-152,392,233 ESR1
    nsv6817297copy number variation1nstd229human GRCh38 chr6: 151,370,892-151,716,763 , GRCh37.p13 chr6: 151,692,027-152,037,898 ARMT1, HSPA8P15, 6 more genes
    nsv6817202copy number variation1nstd229human GRCh38 chr6: 151,908,935-153,594,597 , GRCh37.p13 chr6: 152,230,070-153,915,732 C11orf98P2, RNA5SP225, 18 more genes
    nsv6816610copy number variation1nstd229human GRCh38 chr6: 152,106,555-152,106,687 , GRCh37.p13 chr6: 152,427,690-152,427,822 ESR1
    nsv6816321copy number variation1nstd229human GRCh38 chr6: 151,991,660-151,999,363 , GRCh37.p13 chr6: 152,312,795-152,320,498 ESR1
    nsv6814925copy number variation1nstd229human GRCh38 chr6: 151,673,767-151,676,317 , GRCh37.p13 chr6: 151,994,902-151,997,452 ESR1
    nsv6814227copy number variation1nstd229human GRCh38 chr6: 152,087,342-152,140,012 , GRCh37.p13 chr6: 152,408,477-152,461,147 ESR1, SYNE1
    nsv6813985copy number variation1nstd229human GRCh38 chr6: 152,083,877-152,085,979 , GRCh37.p13 chr6: 152,405,012-152,407,114 ESR1
    nsv6813961copy number variation1nstd229human GRCh38 chr6: 151,849,901-151,854,300 , GRCh37.p13 chr6: 152,171,036-152,175,435 ESR1
    nsv6813949copy number variation1nstd229human GRCh38 chr6: 151,982,329-151,990,638 , GRCh37.p13 chr6: 152,303,464-152,311,773 ESR1
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